참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 4-Vinylphenol | HCID 62453 | — |
| 반응물 | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| 반응물 | p-Hydroxystyrene p-tert-butoxystyrene | HCID 68598693 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | p-1-Ethoxyethoxystyrene p-hydroxystyrene p-tert-butoxystyrene | HCID 131721427 | — |
반응 단계
Poly(p-tert-butoxystyrene) obtained in the same manner as described in Production Example 1(1) in an amount of 15.0 g was suspended in isopropanol and added with 15 ml of concentrated hydrochloric acid. The reaction was carried out at 70° to 80° C. for 4 hours with stirring. After cooling, the reaction solution was poured into 1000 ml of water to deposit crystals. The deposited crystals were filtered, washed with water and dried under reduced pressure to give 9.4 g of white powdered crystals of poly(p-hydroxystyrene/p-tert-butoxystyrene). The proportion of the p-hydroxystyrene unit and the p-tert-butoxystyrene unit of the obtained polymer was about 30:64:6 measured by 1H NMR. Mw was about 17,500 and the degree of dispersion was 1.16 (GPC method, polystyrene standard).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06033826 |
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| 출처 데이터셋 | uspto-grants-2000_03 |
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| ORD ID | ord-cb49ff37dc9b429a91025d15adc62fb4 |
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| 출처 메모 | uspto-grants-2000_03 |
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